Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs886040965
rs886040965
2 0.925 0.040 5 122075443 missense variant C/A snv 0.800 1.000 2 2016 2016
dbSNP: rs886040967
rs886040967
2 0.925 0.040 5 122075482 missense variant T/G snv 0.800 1.000 2 2016 2016
dbSNP: rs876657852
rs876657852
2 0.925 5 122074155 missense variant A/C snv 0.800 0